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Data / Medical devices / China / Hunan Qinghaopuzhong Technology Co., Ltd.

Hunan Qinghaopuzhong Technology Co., Ltd.: FDA-registered device maker in Zhuzhou Hunan, China, 1 510(k) clearance

Hunan Qinghaopuzhong Technology Co., Ltd. is registered with the FDA (registration 3033848620) in Zhuzhou Hunan, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 30, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3033848620
Address
1-3F, Building 2.2- F, Xinma Power Innovation Park, No.899 Xianyue Ring Road, Majiahe Street, Tianyuan Distric, Zhuzhou Hunan, China, 412007
Owner or operator
Hunan Qinghao Puzhong Technology Co., Ltd. (10091348)
Roles
Manufacturer
First device listed
October 24, 2024
Registered through
2026
Brand names listed
Dental Zirconia Blank

Devices it lists

DeviceProduct codeClassRoleSource
Powder, PorcelainEIH2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 30, 2024K241602Kingcera Dental Zirconia BlankEIHSubstantially EquivalentHunan Qinghao Puzhong Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 30, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.